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Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA

Fluorescence microscopy allows specific target detection down to the level of single molecules and has become an enabling tool in biological research. To transduce the biological information to an imageable signal, we have developed a variety of fluorescent probes, such as organic dyes or fluorescen...

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Autores principales: Woehrstein, Johannes B., Strauss, Maximilian T., Ong, Luvena L., Wei, Bryan, Zhang, David Y., Jungmann, Ralf, Yin, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479647/
https://www.ncbi.nlm.nih.gov/pubmed/28691083
http://dx.doi.org/10.1126/sciadv.1602128
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author Woehrstein, Johannes B.
Strauss, Maximilian T.
Ong, Luvena L.
Wei, Bryan
Zhang, David Y.
Jungmann, Ralf
Yin, Peng
author_facet Woehrstein, Johannes B.
Strauss, Maximilian T.
Ong, Luvena L.
Wei, Bryan
Zhang, David Y.
Jungmann, Ralf
Yin, Peng
author_sort Woehrstein, Johannes B.
collection PubMed
description Fluorescence microscopy allows specific target detection down to the level of single molecules and has become an enabling tool in biological research. To transduce the biological information to an imageable signal, we have developed a variety of fluorescent probes, such as organic dyes or fluorescent proteins with different colors. Despite their success, a limitation on constructing small fluorescent probes is the lack of a general framework to achieve precise and programmable control of critical optical properties, such as color and brightness. To address this challenge, we introduce metafluorophores, which are constructed as DNA nanostructure–based fluorescent probes with digitally tunable optical properties. Each metafluorophore is composed of multiple organic fluorophores, organized in a spatially controlled fashion in a compact sub–100-nm architecture using a DNA nanostructure scaffold. Using DNA origami with a size of 90 × 60 nm(2), substantially smaller than the optical diffraction limit, we constructed small fluorescent probes with digitally tunable brightness, color, and photostability and demonstrated a palette of 124 virtual colors. Using these probes as fluorescent barcodes, we implemented an assay for multiplexed quantification of nucleic acids. Additionally, we demonstrated the triggered in situ self-assembly of fluorescent DNA nanostructures with prescribed brightness upon initial hybridization to a nucleic acid target.
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spelling pubmed-54796472017-07-07 Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA Woehrstein, Johannes B. Strauss, Maximilian T. Ong, Luvena L. Wei, Bryan Zhang, David Y. Jungmann, Ralf Yin, Peng Sci Adv Research Articles Fluorescence microscopy allows specific target detection down to the level of single molecules and has become an enabling tool in biological research. To transduce the biological information to an imageable signal, we have developed a variety of fluorescent probes, such as organic dyes or fluorescent proteins with different colors. Despite their success, a limitation on constructing small fluorescent probes is the lack of a general framework to achieve precise and programmable control of critical optical properties, such as color and brightness. To address this challenge, we introduce metafluorophores, which are constructed as DNA nanostructure–based fluorescent probes with digitally tunable optical properties. Each metafluorophore is composed of multiple organic fluorophores, organized in a spatially controlled fashion in a compact sub–100-nm architecture using a DNA nanostructure scaffold. Using DNA origami with a size of 90 × 60 nm(2), substantially smaller than the optical diffraction limit, we constructed small fluorescent probes with digitally tunable brightness, color, and photostability and demonstrated a palette of 124 virtual colors. Using these probes as fluorescent barcodes, we implemented an assay for multiplexed quantification of nucleic acids. Additionally, we demonstrated the triggered in situ self-assembly of fluorescent DNA nanostructures with prescribed brightness upon initial hybridization to a nucleic acid target. American Association for the Advancement of Science 2017-06-21 /pmc/articles/PMC5479647/ /pubmed/28691083 http://dx.doi.org/10.1126/sciadv.1602128 Text en Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Woehrstein, Johannes B.
Strauss, Maximilian T.
Ong, Luvena L.
Wei, Bryan
Zhang, David Y.
Jungmann, Ralf
Yin, Peng
Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title_full Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title_fullStr Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title_full_unstemmed Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title_short Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA
title_sort sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from dna
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479647/
https://www.ncbi.nlm.nih.gov/pubmed/28691083
http://dx.doi.org/10.1126/sciadv.1602128
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